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6-Methyl-3-methylene-5-hepten-2-ol | 127022-73-5

中文名称
——
中文别名
——
英文名称
6-Methyl-3-methylene-5-hepten-2-ol
英文别名
6-methyl-3-methylene-hept-5-en-2-ol;6-Methyl-3-methylen-hept-5-en-2-ol;6-Methyl-3-methylidenehept-5-en-2-ol
6-Methyl-3-methylene-5-hepten-2-ol化学式
CAS
127022-73-5
化学式
C9H16O
mdl
——
分子量
140.225
InChiKey
XGVDTOBNCGOOFO-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    2.8
  • 重原子数:
    10
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

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文献信息

  • .beta.-Stannyl Allylic Alcohols through Photooxygenation (Schenck Reaction) of Vinylstannanes and Reduction of the Resulting Allylic Hydroperoxides: Synthesis and Selected Transformations
    作者:Waldemar Adam、Peter Klug
    DOI:10.1021/jo00089a010
    日期:1994.5
    beta-Stannyl allylic alcohols 2 were prepared regioselectively by photooxygenation (Schenck reaction) of the vinylstannanes 1 and subsequent;reduction of the resulting allylic hydroperoxides by sodium borohydride. This novel methodology makes the hitherto unknown oxyfunctionalized cyclic vinylstannanes conveniently accessible, which constitute valuable building blocks in organic synthesis. For example, palladium-catalyzed coupling of these vinylstannanes 2 with allylic and vinylic halides produced the P-substituted allylic alcohols 3 in good yields. Tin-lithium exchange directly on the oxyfunctionalized vinylstannanes 2 afforded the corresponding lithio dianions, which on reaction with aldehydes led to the allylic diols 4. Furthermore, iododestannylation of the beta-stannyl allylic alcohols 2 gave the respective vinyl iodides 5.
  • Nickel-catalyzed regioselective allylation of allylic alcohols
    作者:Akira Yanagisawa、Nobuyoshi Nomura、Shigeki Habaue、Hisashi Yamamoto
    DOI:10.1016/s0040-4039(01)93908-5
    日期:1989.1
  • Schinz; Bourquin, Helvetica Chimica Acta, 1942, vol. 25, p. 1610
    作者:Schinz、Bourquin
    DOI:——
    日期:——
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